NEDD8-MDP1

NEDD8-MDP1 readthrough E9PL57 E9PL57_HUMAN*
Protein Coding Chr 14 14q12 TrEMBL Entrez 100528064
Mutations
77
CL 12 · Tissue 65
Samples
75
CL 12 · Tissue 63
Peptides
58
unique mutant peptides
Transcripts
1
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations771265
Samples751263
Peptides581150

Function

NEDD8-MDP1 · NEDD8-MDP1 readthrough

This locus represents naturally occurring read-through transcription between the neighboring NEDD8 (neural precursor cell expressed, developmentally down-regulated 8) and MDP1 (magnesium-dependent phosphatase 1) genes on chromosome 14. One of the read-through transcripts on this locus encodes a fusion protein that shares sequence identity with the products of each individual gene. [provided by RefSeq, Jul 2016].

Isoforms & Proteins

1 transcript · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000534348 E9PL57* 77 58

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q12
Entrez ID

Recurrent Mutations

All 58 amino-acid changes on canonical ENST00000534348 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in NEDD8-MDP1 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in NEDD8-MDP1 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Endometrial Carcinoma
1/42 2%
4/612 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Osteosarcoma
1/45 2%
0/166 0%
Medulloblastoma
0/0 0%
2/450 0%
Non-Cancerous
0/104 0%
4/830 0%
Non-Small Cell Lung Carcinoma
2/304 1%
4/1390 0%
Colorectal Carcinoma
2/143 1%
9/3239 0%
Breast Carcinoma
3/144 2%
8/3264 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Melanoma
0/210 0%
6/1899 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Glioma
0/52 0%
2/2127 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%

Mutation Distribution

Where NEDD8-MDP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NEDD8-MDP1 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

Mutations

All 77 mutations in NEDD8-MDP1

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide